A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing

Deep resequencing of functional regions in human genomes is key to identifying potentially causal rare variants for complex disorders. Here, we present the results from a large-sample resequencing (n = 285 patients) study of candidate genes coupled with population genetics and statistical methods to...

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Detalles Bibliográficos
Autores principales: Myers, Rachel A., Casals, Ferran, Gauthier, Julie, Hamdan, Fadi F., Keebler, Jon, Boyko, Adam R., Bustamante, Carlos D., Piton, Amelie M., Spiegelman, Dan, Henrion, Edouard, Zilversmit, Martine, Hussin, Julie, Quinlan, Jacklyn, Yang, Yan, Lafrenière, Ronald G., Griffing, Alexander R., Stone, Eric A., Rouleau, Guy A., Awadalla, Philip
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044677/
https://www.ncbi.nlm.nih.gov/pubmed/21383861
http://dx.doi.org/10.1371/journal.pgen.1001318

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044677/
https://www.ncbi.nlm.nih.gov/pubmed/21383861
http://dx.doi.org/10.1371/journal.pgen.1001318

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